Found: 18
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Rare GPR37L1 Variants Reveal Potential Association between GPR37L1 and Disorders of Anxiety and Migraine.
- Published in:
- Journal of Neuroscience, 2024, v. 44, n. 19, p. 1, doi. 10.1523/JNEUROSCI.1226-23.2024
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- Publication type:
- Article
OikoBase: a genomics and developmental transcriptomics resource for the urochordate Oikopleura dioica.
- Published in:
- Nucleic Acids Research, 2013, v. 41, p. D845, doi. 10.1093/nar/gks1159
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- Publication type:
- Article
Profiles of Extracellular miRNA in Cerebrospinal Fluid and Serum from Patients with Alzheimer's and Parkinson's Diseases Correlate with Disease Status and Features of Pathology.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0094839
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- Publication type:
- Article
Paired Tumor and Normal Whole Genome Sequencing of Metastatic Olfactory Neuroblastoma.
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- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037029
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- Publication type:
- Article
Modeling and analysis of molecularinteraction between Smurf1-WW2 domain and various isoforms of LIM mineralization protein.
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- Proteins, 2007, v. 68, n. 3, p. 690, doi. 10.1002/prot.21429
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- Publication type:
- Article
Artificial intelligence and leukocyte epigenomics: Evaluation and prediction of late-onset Alzheimer's disease.
- Published in:
- PLoS ONE, 2021, v. 16, n. 3, p. 1, doi. 10.1371/journal.pone.0248375
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- Publication type:
- Article
Genetic susceptibility to cerebrovascular disease: A systematic review.
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- Journal of Cerebral Blood Flow & Metabolism, 2018, v. 38, n. 11, p. 1853, doi. 10.1177/0271678X18797958
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- Publication type:
- Article
Comparative proteome analysis of psychrophilic versus mesophilic bacterial species: Insights into the molecular basis of cold adaptation of proteins.
- Published in:
- BMC Genomics, 2009, v. 10, p. 1, doi. 10.1186/1471-2164-10-11
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- Publication type:
- Article
micro RNA changes in liver tissue associated with fibrosis progression in patients with hepatitis C.
- Published in:
- Liver International, 2016, v. 36, n. 3, p. 334, doi. 10.1111/liv.12919
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- Publication type:
- Article
Genome inventory and analysis of nuclear hormone receptors in Tetraodon nigroviridis.
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- Journal of Biosciences, 2007, v. 32, n. 1, p. 43, doi. 10.1007/s12038-007-0005-4
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- Publication type:
- Article
Hidden Burden of Electronic Health Record-Identified Familial Hypercholesterolemia: Clinical Outcomes and Cost of Medical Care.
- Published in:
- 2019
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- Publication type:
- journal article
Large-scale exome datasets reveal a new class of adaptor-related protein complex 2 sigma subunit (AP2σ) mutations, located at the interface with the AP2 alpha subunit, that impair calcium-sensing receptor signalling.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 5, p. 901, doi. 10.1093/hmg/ddy010
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- Publication type:
- Article
Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population.
- Published in:
- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0504-9
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- Publication type:
- Article
Assessment of Probable Opioid Use Disorder Using Electronic Health Record Documentation.
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- JAMA Network Open, 2020, v. 3, n. 9, p. e2015909, doi. 10.1001/jamanetworkopen.2020.15909
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- Publication type:
- Article
Artificial Intelligence and Circulating Cell-Free DNA Methylation Profiling: Mechanism and Detection of Alzheimer's Disease.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 11, p. 1744, doi. 10.3390/cells11111744
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- Publication type:
- Article
Placental cytochrome P450 methylomes in infants exposed to prenatal opioids: exploring the effects of neonatal opioid withdrawal syndrome on health horizons.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2023.1292148
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- Publication type:
- Article
Placental microRNA methylome signatures may serve as biomarkers and therapeutic targets for prenatally opioid-exposed infants with neonatal opioid withdrawal syndrome.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1215472
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- Publication type:
- Article